Neoadjuvant approach as a platform for treatment personalization: focus on HER2-positive and triple-negative breast cancer

被引:41
作者
Miglietta, Federica [1 ,2 ]
Dieci, Maria Vittoria [1 ,2 ]
Griguolo, Gaia [1 ,2 ]
Guarneri, Valentina [1 ,2 ]
机构
[1] Univ Padua, Dept Surg Oncol & Gastroenterol, Padua, Italy
[2] Ist Oncol Veneto IOV IRCCS, Med Oncol 2, Padua, Italy
关键词
Neoadjuvant treatment; Treatment personalization; Triple-negative breast cancer; Biomarkers; HER2+breast cancer; TUMOR-INFILTRATING LYMPHOCYTES; PATHOLOGICAL COMPLETE RESPONSE; RANDOMIZED PHASE-II; OPEN-LABEL; RESIDUAL DISEASE; ADJUVANT TRASTUZUMAB; SECONDARY ANALYSIS; SURVIVAL OUTCOMES; WEEKLY PACLITAXEL; PLUS TRASTUZUMAB;
D O I
10.1016/j.ctrv.2021.102222
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The neoadjuvant setting provides unquestionable clinical benefits for high-risk breast cancer (BC) patients, mainly in terms of expansion of locoregional treatment options and prognostic stratification. Additionally, it is also emerging as a strategical tool in the research field. In the present review, by focusing on HER2-positive and triple-negative subtypes, we examined the role of the neoadjuvant setting as a research platform to facilitate and rationalize the placement of escalation strategies, promote the adoption of biomarker-driven approaches for the investigation of de-escalated treatments, and foster the conduction of comprehensive translational analyses, thus ultimately aiming at pursuing treatment personalization. The solid prognostic role of pathologic complete response after neoadjuvant therapy, and its use as a surrogate endpoint to accelerate the drug approval process were discussed. In this context, available data on escalated treatment strategies capable of enhancing pathologic complete response (pCR) rate or improving prognosis of patients with residual disease (RD) after neoadjuvant treatment, were comprehensively reviewed. We also summarized evidence regarding the possibility of obtaining pCR with de-escalated strategies, with particular emphasis on the role of biomarker-driven approaches for patient selection. Pitfalls of the dichotomy of pCR/RD were also deepened, and data on alternative/complementary biomarkers with a possible clinical relevance in this regard were reviewed.
引用
收藏
页数:13
相关论文
共 104 条
[1]  
Abe O, 2005, LANCET, V366, P2087, DOI 10.1016/s0140-6736(05)66544-0
[2]   A randomized phase II trial of platinum salts in basal-like breast cancer patients in the neoadjuvant setting. Results from the GEICAM/2006-03, multicenter study [J].
Alba, E. ;
Chacon, J. I. ;
Lluch, A. ;
Anton, A. ;
Estevez, L. ;
Cirauqui, B. ;
Carrasco, E. ;
Calvo, L. ;
Segui, M. A. ;
Ribelles, N. ;
Alvarez, R. ;
Sanchez-Munoz, A. ;
Sanchez, R. ;
Lopez Garcia-Asenjo, J. A. ;
Rodriguez-Martin, C. ;
Escudero, M. J. ;
Albanell, J. .
BREAST CANCER RESEARCH AND TREATMENT, 2012, 136 (02) :487-493
[3]   Comparisons between different polychemotherapy regimens for early breast cancer: meta-analyses of long-term outcome among 100 000 women in 123 randomised trials [J].
Albain, K. ;
Anderson, S. ;
Arriagada, R. ;
Barlow, W. ;
Bergh, J. ;
Bliss, J. ;
Buyse, M. ;
Cameron, D. ;
Carrasco, E. ;
Clarke, M. ;
Correa, C. ;
Coates, A. ;
Collins, R. ;
Costantino, J. ;
Cutter, D. ;
Cuzick, J. ;
Darby, S. ;
Davidson, N. ;
Davies, C. ;
Davies, K. ;
Delmestri, A. ;
Di Leo, A. ;
Dowsett, M. ;
Elphinstone, P. ;
Evans, V. ;
Ewertz, M. ;
Gelber, R. ;
Gettins, L. ;
Geyer, C. ;
Goldhirsch, A. ;
Godwin, J. ;
Gray, R. ;
Gregory, C. ;
Hayes, D. ;
Hill, C. ;
Ingle, J. ;
Jakesz, R. ;
James, S. ;
Kaufmann, M. ;
Kerr, A. ;
MacKinnon, E. ;
McGale, P. ;
McHugh, T. ;
Norton, L. ;
Ohashi, Y. ;
Paik, S. ;
Pan, H. C. ;
Perez, E. ;
Peto, R. ;
Piccart, M. .
LANCET, 2012, 379 (9814) :432-444
[4]  
Anders Carey K, 2016, Am Soc Clin Oncol Educ Book, V35, P34, DOI 10.14694/EDBK_159135
[5]   Randomized phase II study of weekly paclitaxel with and without carboplatin followed by cyclophosphamide/epirubicin/5-fluorouracil as neoadjuvant chemotherapy for stage II/IIIA breast cancer without HER2 overexpression [J].
Ando, Masashi ;
Yamauchi, Hideko ;
Aogi, Kenjiro ;
Shimizu, Satoru ;
Iwata, Hiroji ;
Masuda, Norikazu ;
Yamamoto, Naohito ;
Inoue, Kenichi ;
Ohono, Shinji ;
Kuroi, Katsumasa ;
Hamano, Tetsutaro ;
Sukigara, Tamie ;
Fujiwara, Yasuhiro .
BREAST CANCER RESEARCH AND TREATMENT, 2014, 145 (02) :401-409
[6]  
[Anonymous], 2020, PATH COMPL RESP NEOA
[7]   I-SPY 2: An Adaptive Breast Cancer Trial Design in the Setting of Neoadjuvant Chemotherapy [J].
Barker, A. D. ;
Sigman, C. C. ;
Kelloff, G. J. ;
Hylton, N. M. ;
Berry, D. A. ;
Esserman, L. J. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2009, 86 (01) :97-100
[8]  
Bergh J, 2019 ASC ANN M
[9]   Biomarker analysis of the NeoSphere study: pertuzumab, trastuzumab, and docetaxel versus trastuzumab plus docetaxel, pertuzumab plus trastuzumab, or pertuzumab plus docetaxel for the neoadjuvant treatment of HER2-positive breast cancer [J].
Bianchini, Giampaolo ;
Kiermaier, Astrid ;
Bianchi, Giulia Valeria ;
Im, Young-Hyuck ;
Pienkowski, Tadeusz ;
Liu, Mei-Ching ;
Tseng, Ling-Ming ;
Dowsett, Mitch ;
Zabaglo, Lila ;
Kirk, Sarah ;
Szado, Tania ;
Eng-Wong, Jennifer ;
Amler, Lukas C. ;
Valagussa, Pinuccia ;
Gianni, Luca .
BREAST CANCER RESEARCH, 2017, 19
[10]   Impact of immune markers on response to neoadjuvant de-escalated T-DM1 or trastuzumab with/or without endocrine therapy in HR+/HER2+early breast cancer: A translational subproject of the WSG-ADAPT-HER2+/HR+ trial [J].
Biehl, Claudia ;
Kolberg-Liedtke, Cornelia ;
Gluz, Oleg ;
Feuerhake, Friedrich ;
Christgen, Matthias ;
Kates, Ronald ;
Grischke, Eva-Maria ;
Forstbauer, Helmut ;
Braun, Michael ;
Warm, Mathias ;
Hackmann, John ;
Uleer, Christoph ;
Aktas, Bahriye ;
Schumacher, Claudia ;
Kuemmel, Sherko ;
de Haas, Sanne L. ;
Deurloo, Regula ;
Wuerstlein, Rachel ;
Nitz, Ulrike ;
Kreipe, Hans H. ;
Harbeck, Nadia .
CANCER RESEARCH, 2020, 80 (04)